High rate membrane-less microbial electrolysis cell for continuous hydrogen production. Int J Hydrogen Energ

Biotechnology Research Institute, National Research Council of Canada, 6100 Royalmount Avenue, Montreal, QC H2P 2R2, Canada
International Journal of Hydrogen Energy (Impact Factor: 3.31). 01/2009; 34(2):672-677. DOI: 10.1016/j.ijhydene.2008.11.003


This study demonstrates hydrogen production in a membrane-less continuous flow microbial electrolysis cell (MEC) with a gas-phase cathode. The MEC used a carbon felt anode and a gas diffusion cathode with a Pt loading of 0.5 mg cm−2. No proton exchange membrane (PEM) was used in the setup. Instead, the electrodes were separated by a J-cloth. The absence of a PEM as well as a short distance maintained between the electrodes (0.3 mm) resulted in a low internal resistance of 19 Ω. Due to an improved design, the volumetric hydrogen production rate reached 6.3 LSTP d−1. In spite of the PEM absence, methane concentration in the gas collection chamber was below 2.1% and the presence of hydrogen in the anodic chamber was never observed.

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    • "Rozendal et al. [29], Pt loaded carbon felt and gas-diffusion electrodes were employed by Tartakovsky et al. [30], whereas Call and Logan [31] and Selembo et al. [32], used carbon cloth with Pt catalyst. Due to the various disadvantages of Pt like its high cost, environmental impacts due to mining and poisoning by chemicals like sulphide, finding out an alternative for it became a major task. "
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    ABSTRACT: As a reliable source for methane production, the major goal of our research was to design and testify a novel microbial electrolysis assisted upflow anaerobic (Upflow-MEC) reactor for beer wastewater treatment and simultaneous methane production. Three reactors with different cathode materials were constructed and the reactor with Ni cathode had a maximum COD removal of 85%, methane yield of 142.8 mL/gCOD, TOC removal of 83%, Carbohydrate removal of 97%, Protein removal of 62% and current production of 8.6 mA, under 0.8 V applied voltage at HRT of 24 h. It was an application-oriented, membrane-free, continuous reactor and shortening the reaction time and increasing organic content conversion to methane were the key developing targets.
    Full-text · Article · Dec 2015 · International Journal of Hydrogen Energy
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    • "The electrons flow to the cathode through an external wire and combine with protons to form H 2 . The additional energy needed is supplied by an external power supply (Tartakovsky et al. 2009). Although the performance of MECs has improved significantly in recent years, their tests have been limited to the laboratory. "
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    ABSTRACT: The use of commercial electrodes as cathodes in a single-chamber microbial electrolysis cell has been investigated. The cell was operated in sequencing batch mode and the performance of the electrodes was compared with carbon cloth containing 0.5 mg Pt cm(-2). Overall H2 recovery [Formula: see text] was 66.7 ± 1.4, 58.7 ± 1.1 and 55.5 ± 1.5 % for Pt/CC, Ni and Ti mesh electrodes, respectively. Columbic efficiencies of the three cathodes were in the same range (74.8 ± 1.5, 77.6 ± 1.7 and 75.7 ± 1.2 % for Pt/CC, Ni and Ti mesh electrodes, respectively). A similar performance for the three cathodes under near-neutral pH and ambient temperature was obtained. The commercial electrodes are much cheaper than carbon cloth containing Pt. Low cost and good performance of these electrodes suggest they are suitable cathode materials for large scale application.
    Full-text · Article · Jun 2014 · Biotechnology Letters
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    • "Alternatively, it was recently discovered that this thermodynamic barrier may be overcome by means of a small input of electrical energy (Liu et al., 2005b; Rozendal and Buisman, 2005; Rozendal et al., 2006b) in what has been called a microbial electrolysis cell (MEC). More recent developments in bioelectrochemical systems (BESs) suggest that MECs may represent a promising technology for combining wastewater treatment and energy recovery (Ditzig et al., 2007; Logan et al., 2008; Rozendal et al., 2008a,b; Tartakovsky et al., 2009; Pinto et al., 2011) by using the wastewater stream as a free electron supply. "
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    ABSTRACT: Globally, large amounts of electrical energy are spent every year for domestic wastewater (dWW) treatment. In the future, energy prices are expected to rise as the demand for energy resources increases and fossil fuel reserves become depleted. By using appropriate technologies, the potential chemical energy contained in the organic compounds present in dWWs might help to improve the energy and economic balance of dWW treatment plants. Bioelectrochemical Systems (BESs) in general and microbial electrolysis cells (MECs) in particular represent an emerging technology capable of harvesting part of this energy. This study offers an overview of the potential of using MEC technology in dWW treatment plants (dWWTPs) to reduce the energy bill. It begins with a brief account of the basics of BESs, followed by an examination of how MECs can be integrated in dWW treatment plants (dWWTPs), identifying scaling-up bottlenecks and estimating potential energy savings. A simplified analysis showed that the use of MEC technology may help to reduce up to ~20% the energy consumption in a conventional dWWTP. The study concludes with a discussion of the future perspectives of MEC technology for dWW treatment. The growing rates of municipal water and wastewater treatment markets in Europe offer excellent business prospects and it is expected that the first generation of MECs could be ready within 1-4 years. However, before MEC technology may achieve practical implementation in dWWTPs, it needs not only to overcome important techno-economic challenges, but also to compete with other energy-producing technologies.
    Full-text · Article · Jun 2014 · Frontiers in Energy Research
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